GLPBio

S107

Catalog No.: GC19393Purity:>98.00%

S107は、カルスタビン2が変異体および/またはPKAリン酸化されたチャネルに結合する親和性を高めることにより、RyR2チャネルを安定化させるRyR選択的な1,4-ベンゾチアゼピン誘導体です。

製品は研究用途にのみ使用できます。人体には使用できません。患者への販売は行っておりません。


S107
Cas No.: 927871-76-9
10mM (in 1mL DMSO)In Stock
$77.00
1
5mgIn Stock
$70.00
1
10mgIn Stock
$123.00
1
50mgIn Stock
$364.00
1
25mgIn Stock
$245.00
1

引用文献 (Citations)

現在、この製品の引用文献はありません。以下はGlpBio製品を引用した代表的な文献です。
  • Nature cover
    Nature
    641, 529–536 (2025)
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    Nature
    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
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    Science
    387(6739) (2025)
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    Science
    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 273–287 (2023)
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    33, 546–561 (2023)
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    33, 904–922 (2023)
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    Cell Research
    31, 1291–1307 (2021)

製品説明 (Description)

S107 is an orally available, blood-brain barrier-permeable compound that stabilizes RyR2 channels by enhancing the binding of calstabin 2 to the mutant Ryr2-R2474S channel[1]. S107 augments the FKBP12-mediated decrease in channel activity and reverses the harmful effects of redox-active species on sarcoplasmic reticulum (SR) Ca2+ release in skeletal muscle by binding to RyR1 low-affinity sites[2]. S107 has been widely used in preclinical models to prevent ventricular arrhythmias, epileptic seizures, and atrial fibrillation[3].

In vitro, S107 treatment (10µM) for 2h at room temperature restored the intracellular Ca2+ levels and improved contractile properties in cardiomyocytes from Rbm20 knockout rats[4]. Treatment with 10µM S107 for 48 hours rescued the cell dysfunction induced by Aβ42 in mouse hippocampal neurons[5]. Incubation of SH-SY5Y cells with 1µM S107 for 12 hours reduced β-amyloid precursor protein (βAPP) processing, Aβ42 production, and Ca2+ signaling[6].

In vivo, continuous administration of S107 via subcutaneous osmotic pump at a dose of 5mg/kg/h for 7 consecutive days suppressed seizures and improved survival in Ryr2RS/WT mice[1]. Oral administration of S107 (75mg/kg/day) for 21 days effectively alleviated the cognitive decline induced by hindlimb suspension (HU) in C57BL/6NJ mice[7].

References:
[1] Lehnart S E, Mongillo M, Bellinger A, et al. Leaky Ca 2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice[J]. The Journal of clinical investigation, 2008, 118(6): 2230-2245.
[2] Mei Y, Xu L, Kramer H F, et al. Stabilization of the skeletal muscle ryanodine receptor ion channel-FKBP12 complex by the 1, 4-benzothiazepine derivative S107[J]. PloS one, 2013, 8(1): e54208.
[3] Sasaki K, Makiyama T, Yoshida Y, et al. Patient-specific human induced pluripotent stem cell model assessed with electrical pacing validates S107 as a potential therapeutic agent for catecholaminergic polymorphic ventricular tachycardia[J]. PLoS One, 2016, 11(10): e0164795.
[4] Guo W, Zhu C, Yin Z, et al. The ryanodine receptor stabilizer S107 ameliorates contractility of adult Rbm20 knockout rat cardiomyocytes[J]. Physiological Reports, 2021, 9(17): e15011.
[5] Hidisoglu E, Chiantia G, Franchino C, et al. The ryanodine receptor–calstabin interaction stabilizer S107 protects hippocampal neurons from GABAergic synaptic alterations induced by Abeta42 oligomers[J]. The Journal of Physiology, 2022, 600(24): 5295-5309.
[6] Bussiere R, Lacampagne A, Reiken S, et al. Amyloid β production is regulated by β2-adrenergic signaling-mediated post-translational modifications of the ryanodine receptor[J]. Journal of Biological Chemistry, 2017, 292(24): 10153-10168.
[7] Hao J, Zhang Y, Li N, et al. Microgravity‐Induced Cognitive Decline: Investigating the Pathogenic Mechanisms of RyR2 Hyperphosphorylation and S107 Intervention[J]. The FASEB Journal, 2025, 39(13): e70743.

実験プロトコル (Protocol)

Cell experiment [1]:

Cell lines

SH-SY5Y cells expressing the familial double Swedish mutations (APPswe)

Preparation Method

SH-SY5Y cells were cultured in DMEM/F12 medium, supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin, at 37°C in an incubator with 5% CO2. SH-SY5Y cells were treated with S107 (1μM) for 12h, and levels of Aβ and βAPP were measured.

Reaction Conditions

1μM; 12h

Applications

S107 treatment markedly reduced total intracellular Aβ and βAPP levels in SH-SY5Y cells.
Animal experiment [2]:

Animal models

Male C57BL/6NJ mice

Preparation Method

Male C57BL/6NJ mice (6 weeks old; 20±5g) were housed under controlled conditions with a relative humidity of 55%±5%, room temperature maintained at 23°C-24°C, and a 12h light/dark cycle. Food and water were provided ad libitum. Following a 7-day acclimatization period, mice were divided into three groups: control, 7-day HU, and 28-day HU model groups (15-18 mice per group). In the HU groups, mice were tail-suspended with their forelimbs in contact with the ground and their hindlimbs elevated, forming a 30° angle between the body and the ground. Mice were administered S107 at a dose of 75mg/kg/day via drinking water for 21 days. The Morris Water Maze (MWM) was employed to evaluate spatial learning and memory tasks.

Dosage form

75mg/kg/day; 21 days; i.p.

Applications

S107 treatment mitigated the HU-induced cognitive decline in mice.

References:
[1] Bussiere R, Lacampagne A, Reiken S, et al. Amyloid β production is regulated by β2-adrenergic signaling-mediated post-translational modifications of the ryanodine receptor[J]. Journal of Biological Chemistry, 2017, 292(24): 10153-10168.
[2] Hao J, Zhang Y, Li N, et al. Microgravity‐Induced Cognitive Decline: Investigating the Pathogenic Mechanisms of RyR2 Hyperphosphorylation and S107 Intervention[J]. The FASEB Journal, 2025, 39(13): e70743.

製品資料 (Product Documents)

Purity:>98.00%Appearance:A solid

化学的性質 (Chemical Properties)

CAS番号
927871-76-9
SMILES
COC1=CC=C2C(CN(C)CCS2)=C1
分子式
C11H15NOS
分子量
209.31
溶解性
100mg/ml in DMSO
保存条件
Store at -20°C
一般的な注意事項
製品の溶解性データに基づいて適切な溶媒を選択してください。調製後は、凍結融解の繰り返しを避けるため、ストック溶液を小分けしてください。
ストック溶液は、-80°Cで保存する場合は6か月以内、-20°Cで保存する場合は1か月以内に使用してください。
溶解性を高めるには、チューブを37°Cに温め、適切な時間超音波処理してください。
配送条件
評価用サンプルは保冷剤とともに発送します。その他の容量は室温で発送し、ご要望に応じて保冷剤を同梱します。

計算ツール (Calculators)モル濃度 / 希釈 / 分子量 / 単位変換 / in vivo製剤 / 溶解度

g/mol

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